ORIGINAL RESEARCHpublished: 12 June 2017
doi: 10.3389/fphar.2017.00279
Frontiers in Pharmacology | www.frontiersin.org 1 June 2017 | Volume 8 | Article 279
Edited by:
Maria Javier Ramirez,
Universidad de Navarra, Spain
Reviewed by:
Alfredo Briones-Aranda,
Autonomous University of Chiapas,
Mexico
Marcelo Febo,
University of Florida, United States
*Correspondence:
Inge E. M. de Jong
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This article was submitted to
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Frontiers in Pharmacology
Received: 20 February 2017
Accepted: 03 May 2017
Published: 12 June 2017
Citation:
Ferris CF, Kulkarni P, Yee JR,
Nedelman M and de Jong IEM (2017)
The Serotonin Receptor 6 Antagonist
Idalopirdine and Acetylcholinesterase
Inhibitor Donepezil Have Synergistic
Effects on Brain Activity—A Functional
MRI Study in the Awake Rat.
Front. Pharmacol. 8:279.
doi: 10.3389/fphar.2017.00279
The Serotonin Receptor 6 AntagonistIdalopirdine andAcetylcholinesterase InhibitorDonepezil Have Synergistic Effectson Brain Activity—A Functional MRIStudy in the Awake RatCraig F. Ferris 1, Praveen Kulkarni 1, Jason R. Yee 1, Mark Nedelman 2 and
Inge E. M. de Jong 3*
1Department of Psychology, Center for Translational NeuroImaging, Northeastern University, Boston, MA, United States,2 Ekam Imaging, Boston, MA, United States, 3Division of Neurodegeneration, H. Lundbeck A/S, Valby, Denmark
The 5-HT6 receptor is a promising target for cognitive disorders, in particular for
Alzheimer’s disease (AD) and other CNS disorders. The high-affinity and selective 5-
HT6 receptor antagonist idalopirdine (Lu AE58054) is currently in development for
mild-moderate AD as adjunct therapy to acetylcholinesterase inhibitors (AChEIs). We
studied the effects of idalopirdine alone and in combination with the AChEI donepezil
on brain activity using BOLD (Blood Oxygen Level Dependent) functional magnetic
resonance imaging (fMRI) in the awake rat. Idalopirdine (2 mg/kg, i.v.) alone had a
modest effect on brain activity, resulting in activation of eight brain regions at the peak
response. Of these, the cholinergic diagonal band of Broca, the infralimbic cortex, the
ventral pallidum, the nucleus accumbens shell, and the magnocellular preoptic area
were shared with the effects of donepezil (0.3 mg/kg, i.v.). Donepezil alone activated
19 brain regions at the peak response, including several cortical regions, areas of the
septo-hippocampal system and the serotonergic raphe nucleus. When idalopirdine and
donepezil were combined, there was a robust stimulation pattern with activation of
36 brain regions spread across the extended-amygdala-, striato-pallidal, and septo-
hippocampal networks as well as the cholinergic system. These findings indicate that,
whilst idalopirdine and donepezil recruit a number of overlapping regions including one
of the forebrain cholinergic nuclei, the synergistic effect of both compounds extends
beyond the cholinergic system and the effects of donepezil alone toward recruitment of
multiple neural circuits and neurotransmitter systems. These data provide new insight
into the mechanisms via which idalopirdine might improve cognition in donepezil-treated
AD patients.
Keywords: serotonin, acetylcholine, BOLD fMRI, cognition, Alzheimer’s disease
Ferris et al. 5-HT6 Antagonist and Donepezil in Rat fMRI
INTRODUCTION
During the last two decades, the primary approach to thesymptomatic treatment of the cognitive decline in Alzheimer’sdisease (AD) has been represented by the acetylcholinesteraseinhibitors (AChEIs), aiming to relieve the cholinergic deficit byblocking the breakdown of the neurotransmitter acetylcholine(ACh). Although AChEIs improve cognitive function in ADpatients, the benefits are considered modest (Birks and Harvey,2006; Raina et al., 2008; Tan et al., 2014). With the approvalof memantine, an NMDA receptor antagonist addressingglutamatergic dysfunction in AD, a non-cholinergic medicationbecame available which is also increasingly used in combinationwith AChEIs. However, the progressive cognitive decline in ADhas fueled the continued search for novel cognitive enhancersthat may provide symptomatic relief in the face of continuedneuropathology.
The serotonergic system, in particular, has regained interestfor the treatment of cognitive disorders, including AD. The 5-HT6 receptor provides a promising target for the treatment ofcognitive disorders (Meneses et al., 2011; Ramirez, 2013). Thenear exclusive localization in the brain and the predominantexpression in regions that mediate cognition (e.g., hippocampus,cortex, and striatum) have triggered a wealth of studiesinto the therapeutic potential of 5-HT6 receptor ligands(Burton et al., 2015; Calhoun et al., 2017). The procognitiveproperties of antagonists of the 5-HT6 receptor have sincebeen well-documented in preclinical animal models (Mitchelland Neumaier, 2005; Fone, 2008; Arnt et al., 2010; Meneseset al., 2011) that have also suggested a potential benefit ofcombining a 5-HT6 receptor antagonist with an AChEI, as 5-HT6
receptor antagonism was shown to potentiate the neurochemical,electrophysiological, and procognitive effects of the AChEIdonepezil (Marcos et al., 2008; Dawson, 2011; de Bruin et al.,2011). Several 5-HT6 receptor antagonists have now enteredclinical development for the treatment of AD (Maher-Edwardset al., 2011; Wilkinson and Windfeld, 2014; Calhoun et al.,2017; Ferrero et al., 2017). Of these, idalopirdine (Lu AE58054),a high affinity (Ki = 0.83 nm) and selective 5-HT6 receptorantagonist (Arnt et al., 2010), is furthest advanced, and in phaseIII development for the treatment of mild to moderate AD as anadjunct therapy to AChEIs.
The mechanisms via which 5-HT6 receptor antagonismalone, and in combination with an AChEI, mediates
Abbreviations: 5-HT6 receptor, 5-hydroxytryptophan 6 receptor; 5-HT, 5-
hydroxytryptophan (serotonin); ACh, acetylcholine; AChEI, acetylcholinesterase
inhibitor; AD, Alzheimer’s disease; BNST, bed nucleus of the stria terminalis;
BOLD, blood oxygen level dependent; dBB, diagonal band of Broca; EEG,
electroencephalogram; fMRI, functional magnetic resonance imaging; FOV, field
of vision; FWHM, Full Width Half Max; GABA, gamma amino butyric acid; i.v.,
intravenous; MIVA, Medical Image Visualization and Analysis; MS/MS, tandem
mass spectrometry; (m)PFC, (medial) prefrontal cortex; nAcc, nucleus accumbens;
NEX, number of averages; nPO, nucleus pontis oralis; PAG, periaqueductal gray;
p.o., per oral; PPT, pedunculopontine tegmentum; RARE, rapid acquisition with
relaxation enhancement; REM, rapid eye movement; s.c., subcutaneous; SEM,
standard error of means; TE, echo time; Ti-1, inverse transformation matrix; TR,
repetition time.
pro-cognitive effects are not well-understood. Previously,we have demonstrated by in vivo electrophysiology andmicrodialysis that idalopirdine potentiates and prolongs theeffects of donepezil on neuronal oscillations and extracellularlevels of acetylcholine in the rat dorsal hippocampus andprefrontal cortex (Amat-Foraster et al., 2016; Herrik et al.,2016). Such potentiation of the effects of donepezil couldcontribute to the procognitive effects of idalopirdine observedin donepezil-treated AD patients. Further, studies also showedthat idalopirdine monotherapy increases gamma oscillationsand extracellular levels of monoamines and glutamate in therat prefrontal cortex (Amat-Foraster et al., 2016; Mork et al.,2017), suggesting that the effects of idalopirdine extend beyondjust amplification of the effects of donepezil. Indeed, 5-HT6
receptor antagonists have been shown to regulate multipleneurotransmitter systems (reviewed in: Dawson, 2011). Thecellular localization of the receptor, on glutamatergic andGABAergic neurons as well as select populations of GABAergicinterneurons (Helboe et al., 2015), suggests that the 5-HT6
receptor is well-positioned to regulate the balance betweenexcitatory and inhibitory signaling, which may have a broadimpact on brain activity beyond regions where the receptor isexpressed.
To investigate which integrated neural circuits mediate theseparate and combined effects of 5-HT6 receptor antagonismand AChE inhibition on general brain activity, we turned tothe field of functional MRI (fMRI) in awake rodents (Ferriset al., 2011). Awake animal imaging has become an importanttool in preclinical drug discovery (Borsook et al., 2006; Ferriset al., 2011; Haensel et al., 2015). Non-invasive fMRI providesa window to the brain making it possible to image changes inactivity across distributed, integrated neural circuits with hightemporal and spatial resolution. When combined with the useof 3D segmented, annotated, brain atlases, and computationalanalysis, it is possible to reconstruct distributed and integratedneural circuits or “finger prints” of brain activity. These fingerprints may be used to characterize the activity and functionof new psychotherapeutics in preclinical development and tostudy the neurobiology of integrated neural circuits controllingcognition and emotion. To this end, the present study investigatesthe separate and combined effects of 5-HT6 receptor antagonismand AChE inhibition on general brain activity. The imaging datashow a pronounced synergistic effect between idalopirdine anddonepezil that extends across several integrated neural circuitsand different neurotransmitter systems.
METHODS
AnimalsA total of 48 male Sprague Dawley rats (Charles River Labs, MAUSA) were enrolled for use in the study. At study initiation,the rats weighed between 275–350 g and were 3–4 months ofage. The animals were housed in groups of 2 (cage size 30.5 ×
43.2 × 17.8 cm). Animals were maintained in a room with a12-h light/dark cycle (lights on at ∼7:00 A.M.). Temperaturewas maintained at ∼21◦C. Rats were provided water through anautomatic water distribution system (filtered to five microns).
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Food and water were available ad libitum. As part of anenrichment program, animals were provided nylabones, andsunflower seeds for foraging. Upon receipt, rats were acclimatedfor 5 days prior to use in the study. All rats were acquired andcared for in accordance with the guidelines published in theGuide for the Care and Use of Laboratory Animals (NationalInstitutes of Health Publications No. 85–23, Revised 1985) andadhered to the National Institutes of Health and the AmericanAssociation for Laboratory Animal Science guidelines. Theprotocols used in this study were approved by the InstitutionalAnimal Care and Use Committee at the NortheasternUniversity.
AcclimationTo reduce the stress associated with head restraint, rats wereacclimated to the restraining system (head holder and body tube)1 week prior to their actual imaging session. The design ofthe restraining system (Animal Imaging Research, Holden, MA,USA) included a padded head support obviating the need forear bars helping to reduce animal discomfort while minimizingmotion artifact. Rats were briefly anesthetized (∼5–7min) with2–3% isoflurane while being secured into the head holder. Theforepaws were secured with tape. When fully conscious, therestraining system is placed into a black opaque box “mockscanner” for 60min with a tape-recording of the MRI pulsesequence to simulate the bore of the magnet and the imagingprotocol. Rats were acclimated for 5 consecutive days for 60mineach day, and randomly selected to be imaged within 7 days ofthe last acclimation day. The acclimation results in a significantdecline in respiration, heart rate, motor movements, and plasmacorticosterone when the first and last acclimation periods arecompared (King et al., 2005). This reduction in autonomicand somatic measures of arousal and stress improve the signalresolution and quality of the images. Of the 48 rats, fourcontinued to struggle to escape over the 5 day acclimation periodand were excluded from the study. During imaging, an additionalseven were omitted because of motion artifact that could not becorrected and one for electrical interference.
Drug AdministrationFinal group sizes following drug administration were:vehicle (n = 9), idalopirdine (n = 10), donepezil (n = 8),idalopirdine/donepezil (n = 9). All drugs were given i.v.through a tail vein catheter during the imaging session. Ratswere briefly anesthetized with 2–3% isoflurane while beingcatheterized and secured into the head holder. Idalopirdine (LuAE58054, Lundbeck) was dissolved in 5% HpBeta cyclodextrinin distilled water and evaluated at the dose of 2 mg/kg.Donepezil hydrochloride (Lundbeck) was dissolved in 5%HpBeta cyclodextrin in distilled water and evaluated at the doseof 0.3 mg/kg. The combination of idalopirdine (2 mg/kg) anddonepezil (0.3 mg/kg) was also evaluated. The choice of doses inthis single-dose pharmacological study was based on previousstudies that demonstrated that these doses of idalopirdineand donepezil result in clinically relevant exposure of bothcompounds, high 5-HT6 receptor occupancy up to an hourafter administration and synergistic pharmacological effects on
neuronal activity and neurotransmitter release in both the cortexand hippocampus (Amat-Foraster et al., 2016; Herrik et al.,2016; Mork et al., 2017). The vehicle control was 5% HpBetacyclodextrin in distilled water. All injections were given in avolume of 1 ml/kg.
Image AcquisitionAnimals were scanned at 300 MHz using a quadraturetransmit/receive volume coil built into the rat head holderand restraining system for awake animal imaging (AnimalImaging Research, Holden, MA, USA). A video of the ratpreparation for imaging is available at www.youtube.com/watch?v=JQX1wgOV3K4. The design of the coil provided completecoverage of the brain from olfactory bulbs to brain stem.Experiments were conducted using a Bruker Biospec 7.0T/20-cm USR horizontal magnet (Bruker, Billerica, MA, USA) and a20-G/cm magnetic field gradient insert (ID = 12 cm) capable ofa 120-µs rise time. At the beginning of each imaging session,a high-resolution anatomical data set was collected using theRARE pulse sequence (22 slice; 1.0mm; field of vision [FOV]3.0 cm; 256 × 256; repetition time [TR] 2.5 s; echo time [TE] 12ms; NEX (number of averages) 2; ca. 2.5 min acquisition time).Functional images were acquired using a multi-slice HASTEpulse sequence (Half Fourier Acquisition Single Shot Turbo SpinEcho). Bruker Paravision automatically finds the basic frequency,shims, and power requirements for 90◦ and 180◦ pulses and setsthe receiver gain. A single scanning session acquired 22 slices,1.0 mm thick, every 6.0 s (TR 6.0 s, TE 48 ms, FOV 3.0 cm,matrix size 96 × 96, NEX 1) repeated 500 times for a totaltime of 50 min. The in-plane pixel resolution is 312 µm2. Eachscanning session was continuous for 50min, starting with 50baseline image acquisitions during 5 min prior to treatment, thendrug presentation followed by 450 image acquisitions during thefollowing 45 min.
It should also be emphasized that high neuroanatomicalfidelity and spatial resolution are critical in identifyingdistributed neural circuits in any animal imaging study.Many brain areas in a segmented rat atlas have in-planeboundaries of <400 µm2 and may extend for over 1000 µm inthe rostral/caudal plane. With the development of a segmented,annotated 3D MRI atlas for rats (Ekam Solutions, Boston, MA,USA) it is now possible to localize functional imaging data toprecise 3D “volumes of interest” in clearly delineated brainareas. Therefore, it is critical that the functional images are avery accurate reconstruction of the original brain neuroanatomyas shown in Figure 1. To achieve this we used spin echoBOLD (Norris, 2012). The HASTE sequence, a spin-echomultislice pulse sequence, is insensitive to the artifacts of fieldinhomogeneity, susceptibility artifact, chemical shift, and otherimaging distortions. The BOLD signal becomes a function ofdynamic dephasing from diffusion of water at the level of thecapillaries (Duong et al., 2003). Using spin echo BOLD the signalcontrast with BOLD imaging is a function of T2 and not T2∗at high field strengths. The extravascular signal surroundingcapillary beds and small vessels is more reflective of the metabolicchanges in brain parenchyma than signal from large drainingveins helping to improve the localization of the signal changes
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FIGURE 1 | Neuroanatomical fidelity. Representative examples of brain
images collected during a single imaging session using a multi-slice spin echo,
RARE (rapid acquisition with relaxation enhancement) pulse sequence. The
column on the right shows axial sections collected during the anatomical scan
taken at the beginning of each imaging session using a data matrix of 256 ×
256, 22 slices in a field of view of 3.0 cm. The column on the left shows the
same images but collected for functional analysis using HASTE, a RARE pulse
sequence modified for faster acquisition time. These images were acquired
using the same field of view and slice anatomy but a larger data matrix of 96 ×
96. The images in the middle column have been smoothed during
pre-processing. Note the anatomical fidelity between the functional images
and their original anatomical image. The absence of any distortion is necessary
when registering the data to atlas to resolve 171 segmented brain areas.
(Yacoub et al., 2007). The BOLD signal is linear and reproducibleat stimulus intervals of 1 s (Zhang et al., 2009).
Data Analysis/StatisticsFunctional MRI data analysis included four primary steps: (1)preprocessing, including slice timing correction, co-registration,smoothing, and de-trending; (2) registration to rat brain atlas,followed by segmentation; (3) voxel-wise statistical analysis foreach individual to identify voxels that experienced a signal changein relation to baseline; (4) group comparisons on the number ofactivated voxels per ROI and neural network.
Pre-processingPreprocessing of functional scans was performed using in-house MATLAB R© (The Mathworks, Inc, Natick MA.) softwarein combination with SPM8 (http://www.fil.ion.ucl.ac.uk/spm/)batch interface. Slice timing correction was done using SPM 8algorithm (TR = 6 s, slice Order: Interleaved slices, bottom-up,1:2:22, 2:2:22, Reference slice: middle). The mean image of allfunctional time points was computed and using this mean image,the data were roughly cropped slice by slice using a graphicuser interface. This rough cropping insured improved motioncorrection without losing any voxels in the brain. Data wasthen co-registered to a mean functional image using SPM8’s co-registrational code with the following parameters: Quality: 0.97,Smoothing: 0.35 mm, Separation: 0.5 mm. Gaussian smoothingwas performed with a Full Width Half Max kernel width(FWHM) of 0.8 mm. Preprocessed functional files were thenexported to Medical Image Visualization and Analysis (MIVA,EKAM Solutions, available upon request) for registration andsegmentation.
Atlas Registration and SegmentationUsing MIVA, each subject was registered to a segmented ratbrain atlas. Segmentation was performed using a one to onecorrelation to atlas voxels. While segmenting brain regionsspecial care was taken to account for a partial volume effectas described in following ISMRM paper: http://cds.ismrm.org/ismrm-2005/Files/01565.pdf. The alignment process wasfacilitated by an interactive graphic user interface. The affineregistration involved translation, rotation, and scaling in all threedimensions independently. The matrices that transformed thesubject’s anatomy to the atlas space were used to embed each slicewithin the atlas. The mean functional image (output from SPM)was used to register images to the rat atlas since the quality of thefunctional scans are structurally superior to those obtained usinggradient echo (GRE) or echo planar imaging (EPI) sequences asnoted above (see Figure 1). All transformed pixel locations of theanatomical images were tagged with regions in the segmentedatlas creating a fully segmented representation of each subject.
Data AnalysisLow frequency drift is a common problem in time seriesfMRI studies and contributes to signal variability. Instability intemperature regulation with high performance gradients is onepotential source of the problem; however, physiological noise
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and head motion are also considered to be contributing factorsfor drift. The occurrence of false positive voxels is a concernparticularly in the simple off-on activation paradigms used inthese studies comparing the average baseline signal for a givenvoxel to its average post-stimulation signal. This effect may bemore pronounced in longer imaging acquisition times as wasutilized in this study design (∼50 min scans). The data weredetrended by calculating average drift form all segmented voxelsand correcting individual voxels based on average drift. Weassume drift to be linear for all the functional images. Aftersegmentation and brain extraction global drift was computedby calculating average intensity of the whole brain for eachrepetition across the entire scan session. Slope of the data wascomputed with “polyfit” function in Matlab R©; if the slope wasmore than predefined limit (±0.015% signal/ min), then eachindividual voxel was corrected for drift based on computed globalslope. This strategy was adopted over voxel wise drift correctionto avoid overcorrection due to activation in the ROI scans.
In voxel-based analysis, the BOLD % change of eachindependent voxel was computed in its original space. The signalwas filtered for all subjects with a baseline threshold of 2% BOLDchange to account for normal fluctuation of BOLD signal inthe awake rat brain (Brevard et al., 2003). Statistical t-tests wereperformed on each voxel (ca. 15,000 in number) of each subjectwithin their original coordinate system. The average signalintensity in each voxel of the first 5 min of baseline (acquisitions1–50) was compared to minutes 15–25 (acquisitions 150–250),25–35 (acquisitions 250–350), and 35–45 (acquisitions 350–450)post-treatment. t-test statistics with a 95% confidence level, two-tailed distributions, and heteroscedastic variance assumptionswere applied. As a result of themultiple t-test analyses performed,a false-positive detection controlling mechanism was introduced(Genovese et al., 2002). This subsequent filter guaranteed that,on average, p-value of test statistics was below our cutoff of 0.05.A composite image of the whole brain representing the averageof all subjects was constructed for each group for ROI analyses,allowing us to look at each ROI separately to determine theBOLD change and the number of activated voxels in each ROI.Volume of activation was compared across experiment groupsusing the non-parametric Kruskall-Wallis test statistic. Brainareas were considered statistically different between experimentgroups when comparison produced p < 0.05.
Change in BOLD signal over time for each of the experimentalconditions was analyzed using a repeated measures ANOVAfollowed by Dunnett’s post-hoc test which controls for multiplecomparisons of multiple treatment groups to a single controlgroup (“Vehicle”) (Dunnett, 1955). Post-hoc analyses wasconfined to comparisons betweenminutes 15–25, 25–35, and 35–45 post injection for each drug treatment and vehicle tomatch thestatistical comparisons used for the volume of activation data.
RESULTS
Comparison of the Treatments to VehicleTables 1–3 are a selection from 171 brain regions and show onlythose brain regions that are significantly different in volume ofactivation (voxel number) between vehicle and drug treatments
over the entire post treatment period (15–45min). A full listof all 171 brain regions for all treatment comparisons can befound in the Supplementary Data (Supplementary Tables 1–6).Comparison of the acute effect of idalopirdine to vehicle onBOLD signal in 171 brain regions showed little to no significantchanges within the first 15–35 min post-treatment. By 35–45min, idalopirdine showed increased activity in only eight brainregions, three belonging to the mesencephalic dopaminergicsystem (ventral pallidum, accumbens shell, substantia nigra parsreticularis) and one to the basal forebrain cholinergic system(diagonal band of Broca, dBB). In addition, the infralimbiccortex, periaqueductal gray (PAG), medial preoptic area, andmagnocellular preoptic nucleus were activated.
When comparing the acute effect of donepezil to vehicleon BOLD signal, there were 19 brain regions that alreadyshowed significant activation within 15–25 min after treatment(Table 2). These areas included several limbic cortical areas(infralimbic, orbital, insular, frontal association, entorhinal),regions belonging to the septo-hippocampal system (medialseptum, ventral dentate gyrus, entorhinal cortex), the ventralpallidum, and the serotonergic dorsal raphe nucleus. Latertime points evaluated in this study (>25 min followingadministration) showed fewer brain regions significantlyactivated, one of them being the cholinergic dBB.
When comparing the acute effect of the combination ofidalopirdine plus donepezil to vehicle a greater number of brainregions showed significant activation when compared to eitherof the treatments alone. The change in BOLD signal was mostrobust at 25–35 min after treatment, with activation of 36 brainregions (Table 3). The pattern of activation was spread acrossmultiple neural circuits and signaling pathways, including mostof the brain regions that were found activated by one or bothtreatments individually. In addition, it should be emphasizedthat the combination treatment activated more brain regionsthan the addition of those observed with each drug alone.Regions activated by the combination treatment included thecholinergic pendunculopontine tegmentum (PPT), Bed Nucleusof the Stria Terminals (BNST), habenula, anterior cingulatecortex, specific areas of the mesencephalic dopamine system(ventral tegmental area, nucleus accumbens core, prelimbiccortex), amygdala (medial and cortical), septum (triangular,lateral), thalamus (medial dorsal, ventromedial, lateral posterior,and parafascicular), hypothalamus (anterior, posterior, andpremammillary), and olfactory system (granular, glomerular, andexternal plexiform layers of the olfactory bulb, anterior olfactoryn., tenia tecta).
To better organize and visualize the many brain regions andsignaling pathways activated by idalopridine and donepezil aloneand in combination, as reported in Tables 1–3, three integratedneural circuits were defined—the extended-amygdala, striato-pallidal, and septo-hippocampal systems as shown in Figures 2–4(Alheid, 2003). These circuits represent three major cortical-subcortical systems, although it is recognized that they arefunctionally intertwined and that various brain regions could beincluded in many different circuits. Figures 2–4 represent the3D activation maps for each experimental condition (vehicle,idalopirdine alone, donepezil alone, idalopirdine, and donepezil
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TABLE 1 | fMRI BOLD response for idalopirdine compared to vehicle following a single administration.
Vehicle vs. Idalopiridine, postive BOLD volume of activation
15–25 min post-treatment 25–35 min post-treatment 35–45 min post-treatment
Brain area Veh I P-val Brain area Veh I P-val Brain area Veh I P-val
Reuniens nucleus 0 2 0.073 Ventral pallidum 0 5 0.022 Ventral pallidum 0 8 0.006
Ventral pallidum 0 3 0.073 Magnocellular preoptic nucleus 0 1 0.026 Accumbens shell 0 10 0.008
Magnocellular preoptic nucleus 0 0 0.082 Secondary somatosensory ctx 4 32 0.056 Diagonal band of Broca 0 7 0.008
Medial pretectal area 0 0 0.082 Accumbens shell 0 6 0.069 Medial preoptic area 1 8 0.013
Substantia innominata 0 0 0.082 Diagonal band of Broca 0 4 0.092 Infralimbic ctx 0 14 0.015
Accumbens shell 0 4 0.102 Caudal piriform ctx 0 23 0.097 Substantia nigra reticularis 6 17 0.033
Medial septum 0 0 0.114 Supramammillary nucleus 0 1 0.111 Periaqueductal gray thalamus 24 47 0.037
Lateral preoptic area 0 3 0.137 Inferior colliculus 62 85 0.121 Magnocellular preoptic nucleus 0 1 0.042
Shown are three sets of results each representing comparisons between vehicle (Veh, n = 9) and idalopirdine (I, n = 10) treatment groups at times 15–25 (left), 25–35 (middle), and
35–45 (right) min post treatment. The probability values presented on the far-right column were derived using a Kruskall-Wallis test statistic. Lists were generated to include all areas (out
of a total list of 171 areas that comprise the rat MRI atlas) that differed significantly (p < 0.05) for the epoch in which we observed the most changes (i.e., the 35–45 min epoch). Areas
are rank-ordered by p-value for visualization. Areas highlighted in bold differed significantly between treatment groups. Areas listed in gray show areas that come closest to threshold
for statistical significance.
in combination), taken from the 25 to 35 min post-treatmenttime window. These images give an indication of the globalchanges in the networks, whereas the statistical comparisons tovehicle treatment are to be drawn from Tables 1–3. In Figure 2,the 22 3D brain volumes comprising the extended-amygdalasystem are color coded and labeled as shown. These differentbrain regions are coalesced into a single volume (yellow/gold)below showing the localization of the average, significantvolume of activation (red) for each experiment condition. Thispresentation of 3D data in 3D space clearly shows a robustactivation of the extended-amygdala system in response to thecombination treatment including, but not limited to, the brainregions that were activated by idalopirdine and donepezil alone.Whereas the pattern of activity is fairly similar in response toidalopirdine and donepezil alone (donepezil showing greateractivation in the midline hindbrain regions, idalopirdine in theventral CA1 and lateral amygdala), the combination treatmentshows greater activation in the amygdala, nucleus accumbens,prelimbic, and infralimbic areas as well as recruitment of thePPT and the BNST. Shown in Figure 3 are the seventeen 3Dbrain regions that comprise the striato-pallidal system. Foridalopirdine, activation of striatal regions and primary motorcortex stand out, for donepezil it is activation of the habenula.As in Figure 2, the combination treatment shows a greatervolume of activation as compared to the other experimentconditions, with robust activation in the basal ganglia (substantianigra, ventral pallidum, striatum, globus pallidus) and primaryand secondary motor cortices. Shown in Figure 4 are the 203D brain regions that comprise the septo-hippocampal system.In addition, the activation pattern in the septo-hippocampalsystem is represented as 2D data in 2D space (Figure 5), withthe actual location of the average significantly activated voxelsregistered to the rat atlas and in their position in original rawanatomy. Looking across the first row of axial images, note theheightened activation of the septal area with the combinationtreatment. Again, the pattern of activation with the combination
treatment exceeds that of either idalopirdine or donepezil aloneand this pattern of synergistic activity continues through thehippocampal complex as seen in the lower rows of more caudalaxial sections. For example, combining the voxels numbers fordorsal and ventral CA3 (see Supplementary Tables 1–3) showsvehicle with 14 voxels, donepezil with 26 voxels, idalopirdinewith 24 voxels and the combination of both with 48 voxels. Thispattern toward higher activation with the combination treatmentand the location of the activated voxels are visualized in the2D activation maps (Figure 5). However, it should be notedthat the hippocampal complex shows heightened activity for allof the four experiment conditions and, while the combinationtreatment shows the highest volume of activation (voxels) bytwo to three fold, it does not reach significance in the statisticalanalysis when compared to vehicle treatment (Table 3).
Comparison of the Treatments to Vehicleand to Each Other for Bold Signal overTimeShown in Figure 6 are the changes in BOLD signal over the50min imaging session for each drug treatment versus vehiclefor the extended-amygdala system. A repeatedmeasures ANOVAshowed a significant interaction between treatments over time[F(3, 147) = 1.35; p < 0.0001]. Dunnett’s post-hoc analysis at15–25 min showed a significant difference only between thecombination of idalopirdine plus donepezil vs. vehicle (p< 0.05).There were no significant differences for any of the treatmentsat times 25–35 and 35–45. Figure 7 shows the change in BOLDsignal for each treatment in the striato-pallidal system. There wasa statistical trend for the interaction between treatments overtime [F(3, 144) = 1.20, p < 0.063]. Dunnett’s post-hoc analysis at25–35 min showed a statistical trend for the difference betweenthe combination of idalopirdine plus donepezil vs. vehicle (p< 0.10). There were no significant differences for any of thetreatments at other timepoints. Figure 8 shows the change
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TABLE2|fM
RIBOLDresp
onse
fordonepezilcomparedto
vehiclefollowingasingleadministratio
n.
Vehicle
vs.Donepezil,positiveBOLD
volumeofactivity
15–2
5min
post-treatm
ent
25–3
5min
post-treatm
ent
35–4
5min
post-treatm
ent
Brain
area
Veh
DP-val
Brain
area
Veh
DP-val
Brain
area
Veh
DON
P-val
Magnocellularpreopticnucleus
01
0.007
Accumbensshell
05
0.013
Rapheobscurusnucleus
30
0.007
Dorsalraphe
08
0.012
Infralimbic
ctx
010
0.013
Infralimbic
ctx
015
0.01
Medialseptum
03
0.02
Medialseptum
02
0.02
Ventralorbitalctx
07
0.016
Medialorbitalctx
016
0.022
Magnocellularpreopticnucleus
02
0.021
DiagonalbandofBroca
03
0.017
Ventralpallidum
012
0.027
Anteriorolfactory
nucleus
017
0.025
Crus2ofansiform
lobule
39
40.021
Medialgeniculate
022
0.028
Lateralgeniculate
312
0.046
8th
cerebellarlobule
14
00.033
Insularctx
14
107
0.03
Crus2ofansiform
lobule
39
20.047
7th
cerebellarlobule
15
00.04
Superiorcolliculus
29
112
0.03
Ventralo
rbitalctx
04
0.06
Medialp
retectalarea
00
0.051
Frontalassociationctx
010
0.032
Habenulanucleus
319
0.065
Accumbenssh
ell
08
0.052
Inferiorcolliculus
41
108
0.034
Dorsomedialtegmentalarea
02
0.072
Gigantocellularreticularnucleuspons
33
11
0.054
Primary
somatosensory
ctx
upperlip
041
0.041
Diagonalb
andofBroca
04
0.075
6th
cerebellarlobule
46
16
0.054
Dentate
gyrusventral
139
0.043
Medialg
eniculate
114
0.076
Crus1ofansiform
lobule
52
14
0.054
Anteriorolfactory
nucleus
033
0.044
Subiculum
dorsal
626
0.083
Ventralp
allidum
09
0.058
Externalplexiform
layer
23
56
0.047
Entorhinalctx
43
118
0.083
Dorsalraphe
03
0.059
Dorsalparagigantocellularisnucleus
03
0.047
Dorsalraphe
03
0.084
Magnocellularpreoptic
nucleus
01
0.064
Ventralorbitalctx
04
0.048
Peria
queductalg
raythalamus
955
0.092
Paramedianlobule
38
12
0.065
Entorhinalctx
27
147
0.048
Ventralp
allidum
06
0.096
Pontin
enuclei
34
18
0.068
Lateralgeniculate
219
0.049
3rd
cerebellarlobule
417
0.099
Neurallobepitu
itary
63
0.07
Intercalatedamygdaloid
nucleus
00
0.05
Frontalassociatio
nctx
06
0.103
Inferio
rolivary
complex
13
30.076
Shownarethreesetsofresultseachrepresentingcomparisonsbetweenvehicle(Veh,n=9)anddonepezil(D,n=8)treatmentgroupsattimes15–25(left),25–35(middle),and35–45(right)minposttreatment.Theprobabilityvalues
presentedonthefar-rightcolumnwerederivedusingaKruskall-Wallisteststatistic.Listsweregeneratedto
includeallareas(outofatotallistof171areasthatcomprisetheratMRIatlas)thatdifferedsignificantly(p
<0.05)forthe
epochinwhichweobservedthemostchanges(i.e.,the15–25minepoch).Areasarerank-orderedbyp-valueforvisualization.Areashighlightedinbolddifferedsignificantlybetweentreatmentgroups.Areaslistedingrayshowareas
thatcomeclosesttothresholdforstatisticalsignificance.
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Ferris et al. 5-HT6 Antagonist and Donepezil in Rat fMRI
TABLE3|fM
RIBOLDresp
onse
foridalopird
ineplusdonepezilcomparedto
vehiclefollowingasingleadministratio
n.
Vehicle
vs.DonepezilandIdalopiridine,positiveBOLD
volumeofactivity
15–2
5min
post-treatm
ent
25–3
5min
post-treatm
ent
35–4
5min
post-treatm
ent
Brain
area
Veh
I/D
P-val
Brain
area
Veh
I/D
P-val
Brain
area
Veh
I/D
P-val
Magnocellularpreopticnucleus
02
0.012
Infralimbic
ctx
039
0.006
Infralimbic
ctx
028
0.002
Medialpreopticarea
025
0.014
Granularcelllayer
15
81
0.006
Medialorbitalctx
021
0.007
Medialamygdaloid
nucleus
212
0.014
Accumbensshell
013
0.006
Triangularseptalnucleus
310
0.011
Ventralpallidum
015
0.018
Anteriorolfactory
nucleus
033
0.007
Anteriorolfactory
nucleus
132
0.014
Medianraphenucleus
04
0.018
Lateralpreopticarea
08
0.008
Accumbensshell
015
0.016
Anteriorolfactory
nucleus
032
0.019
Habenula
nucleus
318
0.009
Entorhinalctx
51
168
0.017
Ventraltegmentalarea
04
0.03
Ventralpallidum
05
0.009
Ventralpallidum
04
0.018
Posteriorhypothalamic
area
012
0.03
Triangularseptalnucleus
09
0.012
Granularcelllayer
36
75
0.019
Medialdorsalthalamic
nucleus
09
0.031
Medialpreopticarea
026
0.012
Medialpreopticarea
122
0.022
Pedunculopontinetegmentalarea
04
0.033
3rd
cerebellarlobule
422
0.013
Tenia
tecta
ctx
642
0.023
Infralimbic
ctx
019
0.033
Lateralposteriorthalamic
nucleus
845
0.013
Prelimbic
ctx
512
0.026
Ventromedialthalamic
nucleus
011
0.033
Periaqueductalgraythalamus
975
0.013
Medialpretectalarea
00
0.028
Granularcelllayer
22
85
0.034
Accumbenscore
02
0.013
Lateralpreopticarea
06
0.034
Accumbensshell
012
0.034
Medialdorsalthalamic
nucleus
211
0.019
Anteriorcingulate
area
12
59
0.034
Triangularseptalnucleus
15
0.034
Dentate
gyrusventral
424
0.019
Lateralseptalnucleus
16
40
0.034
Tenia
tecta
ctx
646
0.034
Prelimbic
ctx
118
0.023
Magnocellularpreopticnucleus
02
0.035
Corticalamygdaloid
nucleus
11
26
0.037
Lateralseptalnucleus
16
45
0.024
Accumbenscore
02
0.039
Diagonalbandofbroca
04
0.038
Bednucleusstria
term
inalis
214
0.026
Anteriorhypothalamic
area
210
0.049
Lateralpreopticarea
07
0.039
DiagonalbandofBroca
07
0.026
Prim
ary
somatose
nso
ryctx
hindlim
b5
24
0.051
3rd
cerebellarlobule
27
0.04
Medialpretectalarea
00
0.028
Anterio
rpretectaln
ucleus
919
0.051
Medialorbitalctx
015
0.042
Tenia
tecta
ctx
847
0.029
Habenulanucleus
421
0.051
Medialseptum
01
0.044
Posteriorhypothalamic
area
018
0.03
Lateralp
osterio
rthalamicnucleus
23
39
0.052
Reuniensnucleus
02
0.044
Anteriorcingulate
area
450
0.03
Ventralsubiculum
19
50
0.052
Centralm
edialthalamicnucleus
01
0.052
Secondary
somatosensory
ctx
435
0.032
Posterio
rhyp
othalamicarea
215
0.053
Raphelinear
01
0.052
Frontalassociationctx
07
0.032
3rd
cerebellarlobule
715
0.057
Dorsalraphe
04
0.052
Reuniensnucleus
03
0.033
Peria
queductalg
raythalamus
24
48
0.058
Lateralp
osterio
rthalamicnucleus
233
0.057
Primary
somatosensory
ctx
trunk
010
0.033
Diagonalb
andofBroca
07
0.063
Prim
ary
somatose
nso
ryctx
trunk
010
0.058
Magnocellularpreopticnucleus
01
0.035
Extendedamyd
ala
02
0.063
Zonaincerta
016
0.058
Centralgray
27
0.037
Frontalassociatio
nctx
08
0.064
Prim
ary
somatose
nso
ryctx
upperlip
059
0.059
Parafascicularthalamic
nucleus
221
0.037
Mediald
orsalthalamicnucleus
310
0.069
Dentate
gyrusventral
18
0.061
Externalplexiform
layer
29
43
0.038
Medialamyg
daloid
nucleus
514
0.069
Anterio
rhyp
othalamicarea
017
0.065
Glomerularlayer
23
92
0.038
Dentate
gyrusventral
515
0.069
Intercalatedamyg
daloid
nucleus
00
0.067
Ventromedialthalamic
nucleus
06
0.045
Ventrolateralthalamicnucleus
08
0.071
Medialp
retectalarea
00
0.067
Premammillary
nucleus
24
0.048
Corticalamyg
daloid
nucleus
11
24
0.077
Substantia
nigra
reticularis
024
0.072
Dorsomedialtegmentalarea
05
0.05
Reuniensnucleus
03
0.081
Premammillary
nucleus
24
0.073
Primary
somatosensory
ctx
hindlimb
043
0.05
Secondary
motorctx
39
53
0.084
Shownarethreesetsofresultseachrepresentingcomparisonsbetweenvehicle(Veh,n=9)andidalopirdinen/donepezil(I/D,n=9)treatmentgroupsattimes15–25(left),25–35(middle),and35–45(right)minposttreatment.The
probabilityvaluespresentedonthefar-rightcolumnwerederivedusingaKruskall-Wallisteststatistic.Listsweregeneratedtoincludeallareas(outofatotallistof171areasthatcomprisetheratMRIatlas)thatdifferedsignificantly(p
<
0.05)fortheepochinwhichweobservedthemostchanges(i.e.,the25–35minepoch).Areasarerank-orderedbyp-valueforvisualization.Areashighlightedinbolddifferedsignificantlybetweentreatmentgroups.Areaslistedingray
showareasthatcomeclosesttothresholdforstatisticalsignificance.
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Ferris et al. 5-HT6 Antagonist and Donepezil in Rat fMRI
FIGURE 2 | Extended-amygdala system. The 3D color model at the top depicts the location of 22 brain areas in the rat comprising the extended-amygdala system.
These areas have been coalesced into a single volume (yellow) as shown in the lower 3D images for treatment groups, vehicle, idalopirdine, donepezil, and
idalopirdine combined with donepezil. Areas in red are the localization of the activated voxels comprising the composite average from the rats (parentheses) in each
experimental group. Once fully registered and segmented, the statistical responses for each animal are averaged on a voxel-by-voxel basis. Those averaged voxels
that are significantly different from the 5 min baseline for positive BOLD in the 25–35 min post-treatment time window are show in their appropriate spatial location.
in BOLD signal for each treatment in the septo-hippocampalsystem. There was a significant interaction between treatments[F(3, 144) = 1.73; p < 0.012]. Dunnett’s post-hoc analysis at 15–25min showed a significant difference between donepezil vs. vehicle(p < 0.05). There were no significant differences for any of thetreatments at other timepoints.
DISCUSSION
Studies were performed to evaluate how idalopirdine, donepezil,and the combination of both affect brain activity as measured byBOLD MRI in awake rats. A discrete number of brain regionswere significantly activated by both compounds individually,suggesting that they share recruitment of the forebraincholinergic system (dBB), the infralimbic cortex, the ventralpallidum, the nucleus accumbens shell, and the magnocellularpreoptic area. In addition, donepezil activated a number ofcortical regions, the serotonergic dorsal raphe nucleus, and areaswithin the septo-hippocampal system, though remarkably notthe hippocampal complex itself. When both treatments were
combined, there were clear synergistic effects on brain activity,with activation of additional regions within the extended-amygdala, striato-pallidal and septo-hippocampal systems andof the cholinergic PPT. In addition, idalopirdine, alone orin combination with donepezil, may modulate arousal fromexteroceptive (olfactory system) and interoceptive (brainstem)stimuli. Collectively, these data show that the synergistic activityof idalopirdine and donepezil is spread across at least threeintegrated neural networks and includes further activation ofthe cholinergic system. The functional implications of activatingthe brain regions and circuits identified in the current studyremain to be established. In the following paragraphs, wediscuss the potential relevance of these findings with emphasison the procognitive effects of idalopirdine, donepezil, and thecombination of both.
Effects of IdalopirdineWhen reviewing the data from all 171 brain regions forsignificant changes in volume of activity and the BOLD signalchange over time in the three neuronal circuits, few brain
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Ferris et al. 5-HT6 Antagonist and Donepezil in Rat fMRI
FIGURE 3 | Striato-pallidal system. The 3D color model at the top depicts the location of 17 brain areas in the rat comprising the striato-pallidal system. Same as
Figure 2.
regions were significantly activated by idalopirdine alone incomparison to vehicle or the other drug treatments. Of theregions with high-moderate 5-HT6 receptor expression (striatalcomplex, olfactory bulb, hippocampus, cortex), only the nucleusaccumbens shell (ventral striatum) and the infralimbic cortexwere significantly activated. This may indicate that, underthese imaging conditions, there is insufficient serotonergic toneon the 5-HT6 receptor and/or engagement of the associatedneuronal circuits to generate a signal. However, comparison ofthese results with donepezil alone and the combined treatmentsuggests a more complicated set of biological interactions.Indeed, previous studies have shown that some effects of 5-HT6
receptor antagonism require the presence of an AChEI (Dawson,2011; Herrik et al., 2016). The mechanisms underlying thefunctional interaction between an AChEI and a 5-HT6 receptorantagonist are poorly understood, but the current observationthat donepezil activates the dorsal raphe nucleus may indicatethat this AChEI can enhance serotonergic tone.When comparingthe combination treatment to donepezil alone (SupplementaryTable 6), we did observe activation of 5-HT6 receptor-expressing
regions, including multiple striatal regions and the hippocampalCA2 area, indicating that addition of idalopirdine to donepezildoes result in engagement of brain regions with high 5-HT6 receptor expression, which is also supported by the 2and 3D images of the striato-pallidal and septo-hippocampalsystems.
Effects of DonepezilDonepezil alone activated multiple regions of the limbic cortexand the septo-hippocampal system (medial septum, ventraldentate gyrus, and entorhinal cortex), and increased BOLD signalin all three neuronal circuits in discrete time periods, an effectwhich was most pronounced in the septo-hippocampal system.These observations fit well with the mechanism of action and theprocognitive profile of the compound. Indeed, the basal forebraincholinergic system, originating in the medial septum, and thedBB, provides cholinergic innervation to the hippocampus andcortical regions. Donepezil activated both forebrain cholinergicnuclei in the current study and, through inhibition of AChEI,increases the levels of the excitatory neurotransmitter ACh in the
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Ferris et al. 5-HT6 Antagonist and Donepezil in Rat fMRI
FIGURE 4 | Septo-hippocampal system. The 3D color model at the top depicts the location of 21 brain areas in the rat comprising the septo-hippocampal system.
Same as Figure 2.
terminal regions. Remarkably though, the hippocampal complexitself was not significantly activated by donepezil in the presentstudy, which is discussed in more detail below.
Effects of Combination TreatmentThe Cholinergic SystemThe combination treatment activated the PPT, part of the brain-stem cholinergic system, in addition to the basal forebraincholinergic nuclei (medial septum and dBB) that were alsoactivated by donepezil alone or both compounds individually.Electrical stimulation of the PPT has been demonstrated toincrease cortical arousal (Dringenberg and Olmstead, 2003),enhance cortical acetylcholine release (Rasmusson et al., 1994)and facilitate conditioned learning (Andero et al., 2007). Thecurrent finding that the combination treatment activates the PPT,supports our previous observations that idalopirdine potentiatesthe effects of donepezil on cortical extracellular ACh levels andexcitability, manifested as gamma oscillations in the EEG (Amat-Foraster et al., 2016). Indeed, activation of the PPT enhancesgamma oscillatory activity in the cortex through stimulation ofthalamocortical projections (Steriade, 2006).
The PPT (or pendunculopontine nucleus, PPN) also playsa role in the regulation of gait and postural stability and lossof cholinergic neurons in this region is thought to contribute
to deficits in these functions in Parkinson’s disease (PD),parasupranuclear palsy (PSP), and multi systems atrophy (MSA;Bohnen and Albin, 2011; Benarroch, 2013). Consistent with thispossibility, the severity of cholinergic neuronal loss in the PPNcorrelates with the severity of parkinsonian symptoms in PD andlesions involving the PPN manifest with gait disturbances (Azizet al., 1998; Rinne et al., 2008). We have recently demonstratedthat the combination of idalopirdine and donepezil reducesfalls in an animal model of PD with dual dopaminergic andcholinergic lesions (Kucinski et al., 2017). This, together with theactivation of the PPT in the current study, would suggest that thecombination treatment might have beneficial effects on gait andposture through activation of the brainstem cholinergic system.
The Extended-Amygdala SystemThe dopaminergic projections from the VTA to the nucleusaccumbens shell and limbic cortex (including the infralimbic andprelimbic cortices) play a critical role in reward and motivation(Koob, 1996; Malenka et al., 2009). These, as well as other regionsincluded in the extended-amygdala system in the current analysis(several amygdaloid nuclei, BNST, habenula), were activated bythe combination treatment, which also significantly increasedthe BOLD signal as compared to vehicle treatment between 15and 25 min after administration. These observations suggest
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FIGURE 5 | Two dimensional activation maps of the septo-hippocampal system. 2D activation maps from the rat brain atlas showing the precise location of the
significantly altered positive (red) voxels for each of the experimental conditions taken from the 25 to 35 min post-treatment time window in the septo-hippocampal
system. The figures on the right show the localization of the voxels on the original neuroanatomical images for the combined donepezil/idalopirdine condition. The
vertical color strip indicates the percent change in BOLD signal. IDL, idalopirdine; DPZ, donepezil.
an important role for the extended-amygdala system in thecombined effects of idalopirdine and donepezil. Indeed, thereis ample evidence that reward and emotional arousal, in whichthe amygdala plays a central role, contribute to both memoryencoding and consolidation (McGaugh et al., 1996; Phelps andAnderson, 1997; Miendlarzewska et al., 2016). The amygdala alsoplays an important role in the regulation of anxiety and fear.Interestingly, a few studies have suggested that 5-HT6 receptorantagonists may reduce anxiety and depressive-like behavior inrodent models (Wesolowska and Nikiforuk, 2007; Wesolowskaand Jastrzebska-Wiesek, 2011), although the combined effectsof 5-HT6 antagonists with AChEIs have not been tested. Whenregarding the volume of activation, as outlined in Tables 2, 3, anumber of brain regions were activated to a greater extent withthe combination treatment as compared to donepezil alone.
The Striato-Pallidal SystemOf the regions included in the striato-pallidal system, few weresignificantly activated by the individual treatments, with theexception of the substantia nigra pars reticularis by idalopirdineand the ventral pallidum by both treatments individually. Thecombination treatment, in comparison to vehicle, activatedadditional regions within this system but, as described before,not the striatal complex itself. However, when the combinationtreatment was compared to donepezil alone (see SupplementaryTable 6), activation of multiple striatal regions, additionalthalamic nuclei as well as the globus pallidus was observed, whichis supported by the 3D activation maps of the striato-pallidalsystem and the more robust increase in BOLD signal over time as
observed with the combination treatment in the striato-pallidalsystem as a whole.
Recruitment of the striatal-pallidal system may contributeto the procognitive effects of idalopirdine when combined withdonepezil. The ventral striatum, in particular the nucleusaccumbens shell, mediates cognition related to reward,reinforcement, and motivational salience as discussed above. Thedorsal striatum mediates cognition involving stimulus-responselearning, motor function and certain executive functions (Selfand Nestler, 1995; Devan et al., 2011; Daniel and Pollmann,2014). Within the dorsal striatum, the dorsal medial sub-regionmediates goal-directed learning whereas the dorsal lateralstriatum contributes to the acquisition of habits (Yin et al.,2004, 2005a,b; Balleine and O’Doherty, 2010; Liljeholm andO’Doherty, 2012; Burton et al., 2015).
The striato-pallidal system also plays a crucial role inregulation of movement, again depending on the striatal sub-region (Ohno et al., 2011). The current observation that additionof idalopirdine to donepezil results in activation of the dorsallateral striatum, nucleus accumbens core, globus pallidus, andconnected thalamic nuclei, when compared to donepezil alone,suggests engagement of the motor circuitry by the combinationtreatment. This is further supported by the enhanced signal inthe primary and secondary motor cortices with the combinationtreatment in the 3D activation map of the striato-pallidal system.
It is conceivable that activation of the dopaminergic midbrainsystem, specifically the elements that integrate the nigrostriatalpathway, may be related to the factor of restriction of movementthat the rats underwent during the experimental phase, despite
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FIGURE 6 | Time course plots for BOLD in the extended-amygdala system. Shown are the changes in BOLD signal (red) over 45 min (450 image acquisitions) for
each of the different drug treatments as compared to vehicle (black). Each of the 450 time points (drug and vehicle) are the mean of all brain areas in the
extended-amygdala system (see Figure 2). The red time line is segmented into the periods reported in the Tables and show the significant differences between drug
and vehicle at each period. Vertical bars denote SEM.
the fact that all treatment groups were handled equally. Thiscannot be addressed with the current technology as restrictionof movement is a prerequisite for the imaging procedure.
The Septo-Hippocampal SystemThe combination treatment activated several additional regionswithin the septo-hippocampal system (most notably in theseptum), when compared to the effects of donepezil alone.However, neither donepezil nor the combination treatmentsignificantly activated the hippocampal complex itself whencompared to vehicle treatment. This came as a surprise, given thevast literature on the hippocampus, learning and memory, andthe fact that AChEIs were shown to activate the hippocampusand improve hippocampal network connectivity in AD patients(Goekoop et al., 2006; Goveas et al., 2011). However, thecholinergic medial septum/dBB complex, a key modulator ofhippocampal activity and rhythmogenesis, was activated bydonepezil and the combination treatment in the current study
(Dannenberg et al., 2015). Furthermore, we have recentlydemonstrated that donepezil increases hippocampal theta andgamma oscillations during electrical brainstem stimulation inthe anesthetized rat, an effect which was further potentiatedby idalopirdine (Herrik et al., 2016). The apparent discrepancybetween this and the current study may be explained by adifferent level of engagement of the hippocampal formation.In the study by Herrik et al., electrical stimulation of thereticular formation provides heightened afferent input tothe hippocampus, including enhanced cholinergic innervation(Herrik et al., 2016), whereas in the current study the rats, thoughawake, did not receive any salient or cognitively demanding cues.Under the conditions of the fMRI, there may simply not beenough afferent drive to reveal significant effects of donepeziland the combination treatment on hippocampal activity. Inaddition, the current study was performed in young, healthyrats and not in an AD-relevant disease model. The data wouldsuggest the combination treatment engages discrete regions of
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FIGURE 7 | Time course plots for BOLD in the striato-pallidal system. Same as Figure 6.
the septo-hippocampal system which plays a critical role inlearning and memory (Morris et al., 1982; Eichenbaum, 2000;Burgess et al., 2002; Lecourtier et al., 2011), but that theseeffects are not as pronounced as in the extended-amygdala andstriato-pallidal systems under the current conditions of fMRIimaging.
A remarkable finding is that both donepezil and thecombination treatment induced widespread activation in theentorhinal cortex, the region where AD pathology starts andwhich is considered a gate-keeper for the subsequent spreadof AD pathology to the hippocampal formation and corticalregions (Braak and Braak, 1991; Van Hoesen et al., 1991; Khanet al., 2014). In addition, the combination treatment activated theanterior cingulate cortex, a region which has been demonstratedto have reduced metabolism in AD patients with apathy—the most common neuropsychiatric symptom and a symptomassociated with worse prognosis for cognitive and functionalprogression (Marshall et al., 2007; Guimaraes et al., 2008; Stantonet al., 2013; Stella et al., 2014). By increasing activity in theentorhinal and anterior cingulate cortices, the combinationtreatment may enhance function of these brain regions affectedduring the course of AD pathology.
While the drugs included in this study may have effectson peripheral autonomic physiology, especially in the case ofthe AChEI Donepezil, coordination between blood flow andneuronal activity within the brain parenchyma is tightly regulateddue to the high metabolic demand of neuronal tissue. Thus, it isdoubtful that the drug treatments in this study produced theireffects via direct modulation of vascular responses within thebrain parenchyma. However, it is possible that drug treatmentsmodulated peripheral physiology (e.g., noradrenaline activity)thereby initiating an interoceptive cascade that ultimatelyresulted in BOLD changes in the brain. Future studies arerequired to determine whether the drug treatments employed inthis study act through modulation of peripheral physiology.
CaveatsFor any imaging study on awake animals the issues andconsequences related to the stress of head restraint and restrictedbody movement must be considered. Protocols have beendeveloped to help lessen the stress of an imaging study byacclimating animals to the environment of the MR scannerand the restraining devices helping to reduce stress hormoneslevels and measures of sympathetic autonomic activity (Zhang
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Ferris et al. 5-HT6 Antagonist and Donepezil in Rat fMRI
FIGURE 8 | Time course plots for BOLD in the septo-hippocampal system. Same as Figure 6.
et al., 2000; King et al., 2005). These acclimation procedures putanimals through several simulated imaging sessions and havebeen used to study sexual arousal in monkeys (Ferris et al.,2004), generalized seizures in rats and monkeys (Tenney et al.,2003), and exposure to psychostimulants like cocaine (Feboet al., 2004, 2005; Ferris et al., 2005), nicotine (Skoubis et al.,2006), amphetamine (Madularu et al., 2015), and apomorphine(Zhang et al., 2000; Chin et al., 2006). Nonetheless, one mustconsider the experimental confound that exists with low levelsof arousal and stress associated with imaging awake animals.In addition, one must consider the potential effect of earlierexposure to isoflurane during the set-up prior to imaging andthe time that lapses between the final day of acclimation andimaging.
The two measures of BOLD signal change reported here,percent change in BOLD signal over time and volume of
activation, clearly show the synergistic effect of idalopirdine plusdonepezil on brain activity. The change in BOLD signal over timeis the mean of all activated voxels from brain areas comprisingthe neuronal circuit of interest (e.g., 21 areas for the extendedamygdala) while the volume of activation is the number ofsignificantly activated voxels for each of 171 brain areas. Giventhe high level of multiple comparisons the latter method is opento the possibility of false positives and should be considered whenfocusing on any specific brain area.
This study provides insight into the pharmacological effectsof donepezil, idalopirdine and the combination of both on brainactivity in the awake rat. To further study the implicationsof these for AD in particular and cognitive impairment ingeneral, further studies employing animal models capturingneuropathological features of AD and cognitive impairment arecrucial.
Frontiers in Pharmacology | www.frontiersin.org 15 June 2017 | Volume 8 | Article 279
Ferris et al. 5-HT6 Antagonist and Donepezil in Rat fMRI
CONCLUSION
In summary, the current data indicate that, whilst idalopirdineand donepezil recruit a discrete number of overlappingbrain regions including one of the forebrain cholinergicnuclei, the synergistic effect of combining treatment extendsbeyond the effects of donepezil alone and the cholinergicsystem, toward recruitment of multiple neural circuits andneurotransmitter systems. Indeed, the combination treatmentrecruits a constellation of integrated neural circuits associatedwith cognition, emotion and motivation as well as exteroceptive(olfaction) and introceptive cues (brainstem). These maycollectively contribute to enhancing cognition, by enrichinglearning and memory processes with motivational salience andthe context of extro- and intro-ception. These data provide newinsight into how idalopirdine may extend and complement thebenefits of donepezil observed in patients with AD (Wilkinsonand Windfeld, 2014).
AUTHOR CONTRIBUTION
All authors had full access to all the data in the study and takeresponsibility for the integrity of the data and the accuracy of the
data analysis. Study concept and design: Id, CF, MN. Acquisitionof data: CF, PK, MN. Analysis and interpretation of data: CF,PK, JY. Drafting of the manuscript: Id, CF, PK. Critical revisionof the manuscript for important intellectual content: Id, PK,CF. Statistical analysis: PK, CF. Administrative, technical, andmaterial support: PK, JY. Study supervision: Id, CF, MN. Allauthors agree to be accountable for all aspects of the work.
FUNDING
This study was sponsored by H. Lundbeck A/S.
ACKNOWLEDGMENTS
We thank Lone Helboe, Ross Jeggo, Kjartan Herrik, and JanEgebjerg Jensen for critically proof reading the manuscript.
SUPPLEMENTARY MATERIAL
The Supplementary Material for this article can be foundonline at: http://journal.frontiersin.org/article/10.3389/fphar.2017.00279/full#supplementary-material
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Conflict of Interest Statement: CF, PK, and MN have employments at EKAM
imaging. Id is a full-time employee at H. Lundbeck A/S.
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